日期:
2020 年 — 2026 年
2020
2021
2022
2023
2024
2025
2026
影响因子:

Biological and clinical characteristics of ETV6::RUNX1-like ALL

ETV6::RUNX1样急性淋巴细胞白血病的生物学和临床特征

Zaliova, Marketa; Schinnerl, Dagmar; Boer, Judith M; Caye-Eude, Aurélie; Rehn, Jacqueline; Schwab, Claire; Arfeuille, Chloé; Attarbaschi, Andishe; Bergmann, Anke Katharina; Fiser, Karel; de Groot-Kruseman, Hester A; Haslinger, Sabrina; Inthal, Andrea; Janotova, Iveta; Lenk, Lennart; Maurer-Granofszky, Margarita; Nebral, Karin; Poyer, Fiona; Sramkova, Lucie; Stary, Jan; Strullu, Marion; Stuchly, Jan; Sutton, Rosemary; Vaskova, Martina; Winkowska, Lucie; Cario, Gunnar; Cavé, Hélène; den Boer, Monique L; Harrison, Christine; Strehl, Sabine; White, Deborah; Trka, Jan; Zuna, Jan

Epigenetic remodeling via HDAC6 inhibition amplifies anti-tumoral immune responses in myeloid leukemia cells

通过抑制HDAC6进行表观遗传重塑可增强髓系白血病细胞的抗肿瘤免疫反应。

Schliehe-Diecks, Julian; Tu, Jia-Wey; Stachura, Pawel; Schaal, Katerina; Kemkes, Marie; Vasileiou, Eleni; Rüchel, Nadine; Brandes, Danielle; Vogt, Melina; Lenz, Thomas; Nair, Adarsh; Scheu, Stefanie; Dominguez, Pilar M; Pastorczak, Agata; Nebral, Karin; Stühler, Kai; Fischer, Ute; Pandyra, Aleksandra A; Borkhardt, Arndt; Bhatia, Sanil

Transcriptional and epigenetic rewiring by the NUP98::KDM5A fusion oncoprotein directly activates CDK12.

NUP98::KDM5A 融合癌蛋白通过转录和表观遗传重编程直接激活 CDK12

Troester Selina, Eder Thomas, Wukowits Nadja, Piontek Martin, Fernández-Pernas Pablo, Schmoellerl Johannes, Haladik Ben, Manhart Gabriele, Allram Melanie, Maurer-Granofszky Margarita, Scheidegger Nastassja, Nebral Karin, Superti-Furga Giulio, Meisel Roland, Bornhauser Beat, Valent Peter, Dworzak Michael N, Zuber Johannes, Boztug Kaan, Grebien Florian

PAX5::AUTS2 childhood B-ALL: a relapse-prone genetic subtype with frequent central nervous system involvement and a poor outcome

PAX5::AUTS2 儿童 B 细胞急性淋巴细胞白血病:一种易复发的遗传亚型,常累及中枢神经系统,预后不良。

Caye-Eude, Aurélie; Fazio, Grazia; Pastorczak, Agata; Boer, Judith M; Steinemann, Doris; Ganguli, Debdutta; Sonneveld, Edwin; Haslinger, Sabrina; D'Andrea, Lucía; Bradtke, Jutta; Lopes, Bruno A; Zaliova, Marketa; Escherich, Gabriele; König, Margit; Fortschegger, Klaus; Inthal, Andrea; Stasevich, Irina; Emerenciano, Mariana; Trka, Jan; Castillo, Luis; Parihar, Mayur; Moorman, Anthony V; Bergmann, Anke K; den Boer, Monique L; Młynarski, Wojciech; Cazzaniga, Giovanni; Cavé, Hélène; Nebral, Karin; Schinnerl, Dagmar; Strehl, Sabine

A single-center cohort study of patients with hereditary spherocytosis in Central Europe reveals a high frequency of novel disease-causing genotypes

一项针对中欧遗传性球形红细胞症患者的单中心队列研究揭示了新型致病基因型的高频率。

Kager, Leo; Jimenez-Heredia, Raúl; Zeitlhofer, Petra; Novak, Wolfgang; Eder, Sebastian K; Segarra-Roca, Anna; Frohne, Alexandra; Nebral, Karin; Haimel, Matthias; Geyeregger, René; Roetzer-Londgin, Katharina; Haas, Oskar A; Boztug, Kaan

Risk factors in DUX4-positive childhood and adolescent B-cell acute lymphoblastic leukemia

DUX4阳性儿童和青少年B细胞急性淋巴细胞白血病的危险因素

Schinnerl, Dagmar; Riebler, Marion; Schumich, Angela; Haslinger, Sabrina; Bramböck, Alice; Inthal, Andrea; Nykiel, Marek; Maurer-Granofszky, Margarita; Haas, Oskar A; Pötschger, Ulrike; Köhrer, Stefan; Nebral, Karin; Dworzak, Michael N; Attarbaschi, Andishe; Strehl, Sabine

Genomic breakpoint-specific monitoring of measurable residual disease in pediatric non-standard-risk acute myeloid leukemia

对儿童非标准风险急性髓系白血病中可测量的残留疾病进行基因组断点特异性监测

Maurer-Granofszky, Margarita; Kohrer, Stefan; Fischer, Susanna; Schumich, Angela; Nebral, Karin; Larghero, Patrizia; Meyer, Claus; Mecklenbrauker, Astrid; Muhlegger, Nora; Marschalek, Rolf; Haas, Oskar A; Panzer-Grumayer, Renate; Dworzak, Michael N

Erratum to: Genomic breakpoint-specific monitoring of measurable residual disease in pediatric non-standard risk acute myeloid leukemia

勘误:儿科非标准风险急性髓系白血病中可测量残留病灶的基因组断点特异性监测

Maurer-Granofszky, Margarita; Köhrer, Stefan; Fischer, Susanna; Schumich, Angela; Nebral, Karin; Larghero, Patrizia; Meyer, Claus; Mecklenbräuker, Astrid; Mühlegger, Nora; Marschalek, Rolf; Haas, Oskar A; Panzer-Grümayer, Renate; Dworzak, Michael N

Optical Genome Mapping Identifies Novel Recurrent Structural Alterations in Childhood ETV6::RUNX1+ and High Hyperdiploid Acute Lymphoblastic Leukemia

光学基因组图谱鉴定出儿童 ETV6::RUNX1+ 和高超二倍体急性淋巴细胞白血病中新的复发性结构改变

Brandes, Danielle; Yasin, Layal; Nebral, Karin; Ebler, Jana; Schinnerl, Dagmar; Picard, Daniel; Bergmann, Anke K; Alam, Jubayer; Köhrer, Stefan; Haas, Oskar A; Attarbaschi, Andishe; Marschall, Tobias; Stanulla, Martin; Borkhardt, Arndt; Brozou, Triantafyllia; Fischer, Ute; Wagener, Rabea

The KMT2A recombinome of acute leukemias in 2023

2023年急性白血病KMT2A重组组

Meyer, C; Larghero, P; Almeida Lopes, B; Burmeister, T; Gröger, D; Sutton, R; Venn, N C; Cazzaniga, G; Corral Abascal, L; Tsaur, G; Fechina, L; Emerenciano, M; Pombo-de-Oliveira, M S; Lund-Aho, T; Lundán, T; Montonen, M; Juvonen, V; Zuna, J; Trka, J; Ballerini, P; Lapillonne, H; Van der Velden, V H J; Sonneveld, E; Delabesse, E; de Matos, R R C; Silva, M L M; Bomken, S; Katsibardi, K; Keernik, M; Grardel, N; Mason, J; Price, R; Kim, J; Eckert, C; Lo Nigro, L; Bueno, C; Menendez, P; Zur Stadt, U; Gameiro, P; Sedék, L; Szczepański, T; Bidet, A; Marcu, V; Shichrur, K; Izraeli, S; Madsen, H O; Schäfer, B W; Kubetzko, S; Kim, R; Clappier, E; Trautmann, H; Brüggemann, M; Archer, P; Hancock, J; Alten, J; Möricke, A; Stanulla, M; Lentes, J; Bergmann, A K; Strehl, S; Köhrer, S; Nebral, K; Dworzak, M N; Haas, O A; Arfeuille, C; Caye-Eude, A; Cavé, H; Marschalek, R